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A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome
The order Nidovirales is a diverse group of (+)RNA viruses, with a common genome organization and conserved set of replicative and editing enzymes. In particular, RNA methyltransferases play a central role in mRNA stability and immune escape. However, their presence and distribution in different Nid...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638943/ https://www.ncbi.nlm.nih.gov/pubmed/36265859 http://dx.doi.org/10.1093/nar/gkac876 |
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author | Shannon, Ashleigh Sama, Bhawna Gauffre, Pierre Guez, Théo Debart, Françoise Vasseur, Jean-Jacques Decroly, Etienne Canard, Bruno Ferron, François |
author_facet | Shannon, Ashleigh Sama, Bhawna Gauffre, Pierre Guez, Théo Debart, Françoise Vasseur, Jean-Jacques Decroly, Etienne Canard, Bruno Ferron, François |
author_sort | Shannon, Ashleigh |
collection | PubMed |
description | The order Nidovirales is a diverse group of (+)RNA viruses, with a common genome organization and conserved set of replicative and editing enzymes. In particular, RNA methyltransferases play a central role in mRNA stability and immune escape. However, their presence and distribution in different Nidovirales families is not homogeneous. In Coronaviridae, the best characterized family, two distinct methytransferases perform methylation of the N7-guanine and 2′-OH of the RNA-cap to generate a cap-1 structure (m7GpppNm). The genes of both of these enzymes are located in the ORF1b genomic region. While 2′-O-MTases can be identified for most other families based on conservation of both sequence motifs and genetic loci, identification of the N7-guanine methyltransferase has proved more challenging. Recently, we identified a putative N7-MTase domain in the ORF1a region (N7-MT-1a) of certain members of the large genome Tobaniviridae family. Here, we demonstrate that this domain indeed harbors N7-specific methyltransferase activity. We present its structure as the first N7-specific Rossmann-fold (RF) MTase identified for (+)RNA viruses, making it remarkably different from that of the known Coronaviridae ORF1b N7-MTase gene. We discuss the evolutionary implications of such an appearance in this unexpected location in the genome, which introduces a split-off in the classification of Tobaniviridae. |
format | Online Article Text |
id | pubmed-9638943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96389432022-11-07 A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome Shannon, Ashleigh Sama, Bhawna Gauffre, Pierre Guez, Théo Debart, Françoise Vasseur, Jean-Jacques Decroly, Etienne Canard, Bruno Ferron, François Nucleic Acids Res Nucleic Acid Enzymes The order Nidovirales is a diverse group of (+)RNA viruses, with a common genome organization and conserved set of replicative and editing enzymes. In particular, RNA methyltransferases play a central role in mRNA stability and immune escape. However, their presence and distribution in different Nidovirales families is not homogeneous. In Coronaviridae, the best characterized family, two distinct methytransferases perform methylation of the N7-guanine and 2′-OH of the RNA-cap to generate a cap-1 structure (m7GpppNm). The genes of both of these enzymes are located in the ORF1b genomic region. While 2′-O-MTases can be identified for most other families based on conservation of both sequence motifs and genetic loci, identification of the N7-guanine methyltransferase has proved more challenging. Recently, we identified a putative N7-MTase domain in the ORF1a region (N7-MT-1a) of certain members of the large genome Tobaniviridae family. Here, we demonstrate that this domain indeed harbors N7-specific methyltransferase activity. We present its structure as the first N7-specific Rossmann-fold (RF) MTase identified for (+)RNA viruses, making it remarkably different from that of the known Coronaviridae ORF1b N7-MTase gene. We discuss the evolutionary implications of such an appearance in this unexpected location in the genome, which introduces a split-off in the classification of Tobaniviridae. Oxford University Press 2022-10-21 /pmc/articles/PMC9638943/ /pubmed/36265859 http://dx.doi.org/10.1093/nar/gkac876 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Shannon, Ashleigh Sama, Bhawna Gauffre, Pierre Guez, Théo Debart, Françoise Vasseur, Jean-Jacques Decroly, Etienne Canard, Bruno Ferron, François A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome |
title | A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome |
title_full | A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome |
title_fullStr | A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome |
title_full_unstemmed | A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome |
title_short | A second type of N7-guanine RNA cap methyltransferase in an unusual locus of a large RNA virus genome |
title_sort | second type of n7-guanine rna cap methyltransferase in an unusual locus of a large rna virus genome |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638943/ https://www.ncbi.nlm.nih.gov/pubmed/36265859 http://dx.doi.org/10.1093/nar/gkac876 |
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